Chemistry Department, Faculty of Science, University of Kuwait, P.O. Box 5969, Safat 13060, Kuwait.
Molecules. 2013 May 8;18(5):5288-305. doi: 10.3390/molecules18055288.
Chitosan-grafted-poly(4-vinylpyridine) (Cs-PVP) copolymers could be synthesized under heterogeneous conditions in presence of a potassium persulfate and sodium sulfite redox system. The synthesized graft copolymer could be utilized effectively, in the form of beads, as an efficient catalyst for Michael additions of active methylenes to functionally substituted alkenes. Moreover, methyl moiety oxidation in methyl pyridazinyl carbonitriles by H₂O₂ in the presence of chitosan-g-polyvinyl pyridine-supported iron (III) complex, Cs-PVP/Fe, could be affected. A variety of pyrans, naphthopyrans, and thiopyrans could be synthesized efficiently in the presence of these graft copolymer beads by novel catalytic routes. These polymeric catalysts could be used instead of the old toxic commercial organic basic catalysts, piperidine or pyridine, and could be readily isolated from the reaction mixture and recycled several times without significant loss of catalytic activity.
壳聚糖接枝聚(4-乙烯基吡啶)(Cs-PVP)共聚物可以在过硫酸钾和亚硫酸钠氧化还原体系存在的条件下,在非均相条件下合成。合成的接枝共聚物可以有效地用作珠粒形式的高效催化剂,用于活性亚甲基与功能取代烯烃的迈克尔加成反应。此外,壳聚糖接枝聚维酮-负载铁(III)配合物 Cs-PVP/Fe 的存在下,通过 H₂O₂可以影响甲基吡啶基腈基中的甲基部分的氧化。通过这些接枝共聚物珠粒的新型催化途径,可以有效地合成各种吡喃、萘并吡喃和噻吩并吡喃。这些聚合物催化剂可以替代旧的有毒商业有机碱性催化剂,如哌啶或吡啶,并且可以很容易地从反应混合物中分离出来,并在没有显著损失催化活性的情况下重复使用多次。